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DO Term : autosomal recessive osteopetrosis 2 [DOID:0110943] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An osteopetrosis characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the TNFSF11 gene on chromosome 13q14.
  • synonyms:
  • osteoclast-poor osteopetrosis,
  • mild autosomal recessive form osteopetrosis,
  • OMIM:259710,
  • OPTB2,
  • GARD:4157,
  • 259710
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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